TECHNICAL FIELD
[0001] The present invention relates to a reactor module, a liquid fuel synthesis method,
a separation membrane module, and a separation method.
BACKGROUND ART
[0002] In recent years, reactors have been developed that can improve, in a conversion reaction
of a raw material gas containing hydrogen and carbon oxide to a liquid fuel such as
methanol and ethanol (specifically, a fuel that is in a liquid state at normal temperature
and pressure), conversion efficiency by separating water vapor that is generated together
with the liquid fuel.
[0003] For example, Patent Literature 1 discloses a tubular reactor provided with a separation
membrane permeable to water vapor, which is one of the products of the conversion
reaction, a non-permeation side flow path through which a raw material gas flows,
and a permeation side flow path through which a sweep gas flows.
CITATION LIST
Patent Literature
SUMMARY
TECHNICAL PROBLEM
[0005] According to the reactor disclosed in Patent Literature 1, since reaction heat generated
due to the conversion reaction can be removed by causing the sweep gas to flow through
the permeation side flow path, the conversion efficiency can be further improved.
[0006] However, in the reactor disclosed in Patent Literature 1, since the sweep gas flows
through only the permeation side flow path in the reactor, there is a limitation in
removing the reaction heat.
[0007] Also, in a separation membrane module provided with a separation filter, in some
cases, in order to control the separation membrane permeable to a desired component
contained in a mixed fluid to an appropriate temperature, the separation membrane
is to be cooled or heated by causing the sweep gas to flow through the permeation
side flow path.
[0008] An object of the present invention is to provide a reactor module, a liquid fuel
synthesis method, a separation membrane module, and a separation method, capable of
efficiently controlling a temperature.
SOLUTION TO PROBLEM
[0009] A reactor module according to the present invention includes a monolith-type reactor
extending in a longitudinal direction, a housing configured to house the reactor,
an annular first seal portion configured to seal a space between the housing and a
first end portion of the reactor, and an annular second seal portion configured to
seal a space between the housing and a second end portion of the reactor, and an air-permeable
annular flow rate adjustment unit disposed between the first seal portion and the
second seal portion in the longitudinal direction. The reactor includes a separation
membrane permeable to a product of a conversion reaction of a raw material gas containing
hydrogen and carbon oxide to a liquid fuel, a first flow path on a non-permeation
side of the separation membrane, and a second flow path on a permeation side of the
separation membrane. The second flow path includes an inflow port open to a first
space between the first seal portion and the flow rate adjustment unit, and an outflow
port open to a second space between the second seal portion and the flow rate adjustment
unit. The housing includes a supply port for supplying a sweep gas to the first space,
and an exhaust port for discharging the sweep gas from the second space. In a side
view of the reactor, a direction in which the sweep gas flows from the first space
to the second space via the flow rate adjustment unit is the same as a direction in
which the sweep gas flows through the second flow path.
ADVANTAGEOUS EFFECTS
[0010] According to the present invention, it is possible to provide a reactor module, a
liquid fuel synthesis method, a separation membrane module, and a separation method,
capable of efficiently controlling a temperature.
BRIEF DESCRIPTION OF DRAWINGS
[0011]
FIG. 1 is a perspective view of a reactor 1 according to an embodiment.
FIG. 2 is a cross-sectional view taken along A-A in FIG. 1.
FIG. 3 is a cross-sectional view taken along B-B in FIG. 1.
FIG. 4 is a cross-sectional view taken along C-C in FIG. 2.
FIG. 5 is a transparent side view of a reactor module according to the embodiment.
FIG. 6 is a cross-sectional view of the reactor module according to the embodiment.
FIG. 7 is a cross-sectional view of the reactor module according to the embodiment.
FIG. 8 is a cross-sectional view of a flow rate adjustment unit according to Modification
3.
DESCRIPTION OF EMBODIMENTS
[0012] Embodiments of the present invention will be described with reference to the drawings.
However, the drawings are schematic, and ratio or the like of dimensions may differ
from an actual one.
Reactor 1
[0013] FIG. 1 is a perspective view of a reactor 1. FIG. 2 is a cross-sectional view taken
along A-A in FIG. 1. FIG. 3 is a cross-sectional view taken along B-B in FIG. 1. FIG.
4 is a cross-sectional view taken along C-C in FIG. 2.
[0014] A reactor 1 is a so-called membrane reactor used to convert a raw material gas to
a liquid fuel. The raw material gas contains at least hydrogen and carbon oxide. As
the carbon oxide, at least one of carbon monoxide and carbon dioxide can be used.
The raw material gas may be a so-called synthetic gas (syngas). The liquid fuel is
a fuel that is in a liquid state at normal temperature and pressure, or a fuel that
can be liquidized at normal temperature and pressurized state. Examples of the liquid
fuel that is in a liquid state at normal temperature and pressure may include methanol,
ethanol, liquid fuels represented by C
nH
2(m-2n) (m is an integer less than 90, and n is an integer less than 30), and mixtures thereof.
Examples of the fuel that can be liquidized at normal temperature and pressurized
state include, for example, propane, butane, and mixtures thereof.
[0015] For example, reaction formula (1) for synthesizing methanol by catalytically hydrogenating
a raw material gas containing carbon dioxide and hydrogen in the presence of a catalyst
is as follows.
CO
2 + 3H
2 ↔ CH
3OH + H
2O (1)
[0016] The above reaction is an equilibrium reaction, and in order to increase both the
conversion efficiency and the reaction rate, it is preferable to carry out the reaction
at high temperature and high pressure (for example, 180°C or higher and 2 MPa or higher).
The liquid fuel is in a gaseous state when it is synthesized, and is kept in a gaseous
state at least until it flows out of the reactor 1. The reactor 1 preferably has heat
resistance and pressure resistance suitable for desired synthesis conditions of the
liquid fuel.
[0017] As shown in FIG. 1, the reactor 1 is formed in a monolith shape. A monolith means
a shape including a plurality of holes that pass through in a longitudinal direction,
and is a concept including a honeycomb. The reactor 1 extends in the longitudinal
direction. The reactor 1 is formed in a columnar shape. Although the reactor 1 is
formed in a circular columnar shape in the present embodiment, the outer shape of
the reactor 1 is not particularly limited.
[0018] The reactor 1 includes a first end portion 1a and a second end portion 1b. The first
end portion 1a is, when the reactor 1 is equally divided into five in the longitudinal
direction, a portion extending to two-fifths from one end of the reactor 1. The second
end portion 1b is, when the reactor 1 is equally divided into five in the longitudinal
direction, a portion extending to two-fifths from the other end of the reactor 1.
In the present embodiment, the first end portion 1a of the reactor 1 is on a side
to which the raw material gas flows in, and the second end portion 1b of the reactor
1 is on a side from which the liquid fuel flows out.
[0019] The reactor 1 includes a first end face S1, a second end face S2, and a side face
S3. The first end face S1 is an end face on the first end potion 1a side. The second
end face S2 is an end face on the second end potion 1b side. The first end face S1
is provided on the opposite side to the second end face S2. The side face S3 is continuous
with outer edges of the first end face S1 and the second end face S2.
[0020] As shown in FIGS. 1 to 4, the reactor 1 includes a porous support body 10, catalysts
20, separation membranes 30, a first seal portion 40, and a second seal portion 50.
[0021] The porous support body 10 is a columnar body extending in the longitudinal direction
of the reactor 1. The porous support body 10 is constituted by a porous material.
[0022] As the porous material, a ceramic material, a metal material, a resin material, or
the like can be used, and a ceramic material is particularly preferable. As an aggregate
of the ceramic material, for example, at least one of alumina (Al
2O
3), titania (TiO
2), mullite (Al
2O
3-SiO
2), potsherd, cordierite (Mg
2Al
4Si
5O
18) can be used. As an inorganic binder for the ceramic material, for example, at least
one of titania, mullite, readily sinterable alumina, silica, glass frit, a clay mineral,
and readily sinterable cordierite can be used. However, the ceramic material does
not need to contain an inorganic binder.
[0023] As shown in FIGS. 2 and 3, the porous support body 10 includes a number of first
flow paths 11 and a plurality of second flow paths 12.
[0024] As shown in FIG. 4, the first flow paths 11 are formed in the longitudinal direction
of the reactor 1. The first flow paths 11 are located on a non-permeation side of
the separation membranes 30. The raw material gas is caused to flow through the first
flow paths 11. The first flow paths 11 are through holes. The first flow paths 11
are open in the first end face S1 and the second end face S2 of the reactor 1. The
first flow paths 11 each include an inflow port e1 of the raw material gas, formed
in the first end face S1, and an outflow port e2 of the liquid fuel, formed in the
second end face S2.
[0025] The catalysts 20 are respectively disposed in the first flow paths 11. The number,
position, shape, and the like of the first flow paths 11 can be changed as appropriate.
[0026] The second flow paths 12 are located on a permeation side of the separation membranes
30. A sweep gas for sweeping the water vapor that has permeated through the separation
membranes 30 is caused to flow through the second flow paths 12. An inert gas (e.g.,
nitrogen), air, or the like can be used as the sweep gas. In the present embodiment,
which is a heat generation reaction, the temperature of the sweep gas is lower than
an operation temperature of the reactor 1. The number, position, shape, and the like
of the second flow paths 12 can be changed as appropriate.
[0027] Here, as shown in FIGS. 2 and 3, the second flow paths 12 are each formed by a plurality
of cells 13, an inflow slit 14, and an outflow slit 15.
[0028] The plurality of cells 13 are arranged in a row along a short direction (a direction
orthogonal to the longitudinal direction) of the reactor 1. As shown in FIG. 4, the
cells 13 are formed along the longitudinal direction of the reactor 1. Both ends of
each cell 13 are respectively sealed by first and second opening seal portions 17
and 18. The first and second opening seal portions 17 and 18 can be constituted by
the above porous material.
[0029] As shown in FIG. 1, the inflow slits 14 are formed at the first end portion 1a in
the longitudinal direction of the reactor 1. As shown in FIG. 2, the inflow slits
14 are formed along the short direction of the reactor 1. The inflow slits 14 pass
through the plurality of cells 13. Both ends of the inflow slits 14 are open in the
side face S3. The inflow slits 14 each include a pair of inflow ports d1 formed in
the side face S3. The pair of inflow ports d1 correspond to one end of the second
flow paths 12 in the longitudinal direction.
[0030] As shown in FIG. 1, outflow slits 15 are formed in the second end portion 1b of the
reactor 1 in the longitudinal direction. As shown in FIG. 3, the outflow slits 15
are formed along the short direction of the reactor 1. The outflow slits 15 pass through
the plurality of cells 13. Both ends of the outflow slits 15 are open in the side
face S3. The outflow slits 15 each include a pair of outflow ports d2 formed in the
side face S3. The pair of outflow ports d2 correspond to the other ends of the second
flow paths 12 in the longitudinal direction.
[0031] The catalysts 20 are respectively disposed in the first flow paths 11. Although the
catalysts 20 preferably fill the respective first flow paths 11, the catalysts 20
may be respectively disposed on the surfaces of the separation membranes 30 in a layered
manner. As represented by the above formula (1), the catalysts 20 promote the conversion
reaction of the raw material gas to the liquid fuel.
[0032] As the catalysts 20, a known catalyst suitable for the conversion reaction to a desired
liquid fuel can be used. Examples of the catalysts 20 include metal catalysts (copper,
palladium, and the like), oxide catalysts (zinc oxide, zirconia, gallium oxide, and
the like), and composite catalysts thereof (copper-zinc oxide, copper-zinc oxide-alumina,
copper-zinc oxide-chromium oxide-alumina, copper-cobalt-titania, catalysts obtained
by modifying these with palladium, and the like).
[0033] The separation membranes 30 are supported by the porous support body 10. The separation
membranes 30 surround the respective first flow paths 11. The separation membranes
30 are disposed between the first flow paths 11 and the second flow paths 12.
[0034] The separation membranes 30 are permeable to water vapor, which is one of the products
of the conversion reaction of the raw material gas to a liquid fuel. In this manner,
by utilizing the equilibrium shift effect, the reaction equilibrium of the above formula
(1) can be shifted to the product side.
[0035] The separation membrane 30 preferably has a water vapor permeability coefficient
of 100 nmol/(s·Pa·m
2) or more. The water vapor permeability coefficient can be determined using a known
method (see
Ind. Eng. Chem. Res., 40, 163-175 (2001)).
[0036] The separation membrane 30 preferably has a separation factor of 100 or more. The
greater the separation factor is, the more permeable the separation membrane 112 is
to water vapor, and the less permeable it is to components other than water vapor
(e.g., hydrogen, carbon dioxide, and liquid fuel). The separation factor can be determined
using a known method (see FIG. 1 of "
Separation and Purification Technology 239 (2020) 116533").
[0037] An inorganic membrane can be used as the separation membrane 30. The inorganic membrane
is preferable because it has heat resistance, pressure resistance, and water vapor
resistance. Examples of the inorganic membrane include a zeolite membrane, a silica
membrane, an alumina membrane, and a composite membrane thereof. In particular, an
LTA zeolite membrane having a molar ratio (Si/Al) of a silicon element (Si) and an
aluminum element (Al) of 1.0 or more and 3.0 or less is suitable because of its excellent
water vapor permeability.
[0038] As shown in FIG. 1, a first seal portion 40 covers the first end face S1 and part
of the side face S3 of the porous support body 10. The first seal portion 40 suppresses
entry of the raw material gas into the porous support body 10. As shown in FIG. 4,
the first seal portion 40 is formed so as not to close the inflow ports e1 of the
first flow paths 11. The first seal portion 40 covers a first opening seal portion
17. The first seal portion 40 can be constituted by glass, metal, rubber, resin, or
the like.
[0039] As shown in FIG. 1, the second seal portion 50 covers part of the second end face
S2 and the side face S3 of the porous support body 10. The second seal portion 50
suppresses entry of the liquid fuel into the porous support body 10. As shown in FIG.
4, the second seal portion 50 is formed so as not to close the outflow ports e2 of
the first flow paths 11. The second seal portion 50 covers a second opening seal portion
18. The second seal portion 50 can be constituted by glass, metal, rubber, resin,
or the like.
Liquid Fuel Synthesis Method Using Reactor 1
[0040] A liquid fuel synthesis method using the reactor 1 will be described with reference
to FIG. 4.
[0041] The liquid fuel synthesis method using the reactor 1 includes a step of causing the
sweep gas to flow through the second flow paths 12 provided on the permeation side
of the separation membranes 30, while causing the raw material gas to flow through
the first flow paths 11 provided on the non-permeation side of the separation membranes
30.
[0042] The raw material gas flows into the first flow paths 11 through the inflow ports
e1 of the first flow paths 11. In the first flow paths 11, water vapor is generated
together with the liquid fuel in accordance with the above formula (1). The synthesized
liquid fuel flows out through the outflow ports e2 of the first flow paths 11. Water
vapor, which is one of the products, sequentially permeates through the separation
membranes 30 and the porous support body 10, and then moves to the second flow paths
12. Note that the liquid fuel flowing out through the outflow ports e2 may be mixed
with a residual raw material gas that was not used in the conversion reaction, water
vapor, which is one of the products of the conversion reaction, and the like.
[0043] After flowing in through the inflow ports d1 of the inflow slits 14, the sweep gas
flows into the cells 13 through the inflow slits 14. Next, the sweep gas that has
flowed into the cells 13 through the inflow slits 14 takes in water vapor that has
permeated through the separation membranes 30, and flows through the cells 13 toward
the outflow slits 15 while absorbing the reaction heat generated by the conversion
reaction. The sweep gas that has reached the outflow slits 15 flows out through the
outflow ports d2 of the outflow slits 15.
[0044] As shown in FIG. 4, in the present embodiment, in the side view of the separation
membranes 30, the direction in which the sweep gas flows through the second flow paths
12 is the same as the direction in which the raw material gas flows through the first
flow paths 11. That is, the sweep gas flowing through the second flow paths 12 flows
in the direction parallel with the direction in which the raw material gas flows through
the first flow paths 11.
[0045] Note that in the side view of the separation membranes 30, the direction in which
the sweep gas flows through the second flow paths 12 may be opposite to the direction
in which the raw material gas flows through the first flow paths 11. That is, the
sweep gas flowing through the second flow paths 12 may flow in the direction opposite
to the direction in which the raw material gas flows through the first flow paths
11.
Reactor Module 2
[0046] Next, a reactor module 2 according to the embodiment will be described. FIG. 5 is
a transparent side view of the reactor module 2.
[0047] As shown in FIG. 5, the reactor module 2 is provided with the above monolith-type
reactor 1, a housing 3, an annular first seal portion 4, an annular second seal portion
5 and an annular flow rate adjustment unit 6.
[0048] The housing 3 is constituted by a metal material such as a stainless steel. The housing
3 houses the reactor 1. The housing 3 includes a sweep gas supply port 3a, a sweep
gas exhaust port 3b, a raw material gas supply port 3c and a liquid fuel exhaust port
3d. A space inside the housing 3 is partitioned into a first space P1 to a fourth
space P4 by the first seal portion 4, the second seal portion 5, and the flow rate
adjustment unit 6.
[0049] The first space P1 is a space between the first seal portion 4 and the flow rate
adjustment unit 6. Sweep gas inflow ports d1 formed in the side face S3 of the reactor
1 are open to the first space P1. The sweep gas supply port 3a for supplying the sweep
gas to the first space P1 is open to the first space P1. The second space P2 is a
space between the second seal portion 5 and the flow rate adjustment unit 6. Sweep
gas outflow ports d2 formed in the side face S3 of the reactor 1 are open to the second
space P2. The sweep gas exhaust port 3b for discharging the sweep gas from the second
space P2 is open to the second space P2. The first space P1 and the second space P2
are partitioned by the flow rate adjustment unit 6.
[0050] The raw material gas supply port 3c for supplying the raw material gas to the third
space P3 is open to the third space P3. A raw material gas inflow port e1 (see FIG.
4) formed in the first end face S1 of the reactor 1 is open in the third space P3.
The liquid fuel exhaust port 3d for discharging the liquid fuel from the fourth space
P4 is open to the fourth space P4. A liquid fuel outflow port e2 (see FIG. 4) formed
in the second end face S2 of the reactor 1 is open to the fourth space P4. The first
space P1 and the third space P3 are partitioned by the first seal portion 4, and the
second space P2 and the fourth space P4 are partitioned by the second seal portion
5.
[0051] The first seal portion 4 has an annular shape. The first seal portion 4 fixes the
first end portion 1a of the reactor 1 to the housing 3. The first seal portion 4 is
connected to the side face S3 of the reactor 1 and the inner face T1 of the housing
3. The first seal portion 4 seals a space between the first end portion 1a of the
reactor 1 and the housing 3. Examples of the constituent materials of the first seal
portion 4 include glass, silver solder, solder, and inorganic adhesive.
[0052] The second seal portion 5 has an annular shape. The second seal portion 5 fixes the
second end portion 1b of the reactor 1 to the housing 3. The second seal portion 5
is connected to the side face S3 of the reactor 1 and an inner face T1 of the housing
3. Since the fourth space P4 side of the second seal portion 5 is exposed to a high
temperature liquid fuel and water vapor, resistance against chemical load of the high
temperature liquid fuel and resistance against water vapor are required in the constituent
materials of the second seal portion 5. Examples of the constituent materials of the
second seal portion 5 include glass, silver solder, solder, and inorganic adhesive.
Rubber and plastic are not suitable for the constituent materials of the second seal
portion 5.
[0053] The flow rate adjustment unit 6 has an annular shape. The flow rate adjustment unit
6 is disposed between the first seal portion 4 and the second seal portion 5 in the
longitudinal direction. The flow rate adjustment unit 6 partitions between the first
space P1 and the second space P2.
[0054] The flow rate adjustment unit 6 has air permeability. The flow rate adjustment unit
6 can cause the sweep gas to pass through from the first space P1 to the second space
P2. The flow rate adjustment unit 6 is a member for adjusting the flow rate of the
sweep gas flowing from the first space P1 to the second space P2 via the flow rate
adjustment unit 6. The air permeability of the flow rate adjustment unit 6 can be
adjusted by changing the porosity of the material constituting the flow rate adjustment
unit 6, the width of the flow rate adjustment unit 6 in the longitudinal direction,
or the number of flow rate adjustment units 6.
[0055] The flow rate adjustment unit 6 can be constituted by the porous material. The porous
material can be constituted by exfoliated graphite, a porous rubber, a porous resin,
or the like.
[0056] The sweep gas is supplied to the first space P1 through the sweep gas supply port
3a. Some of the sweep gas passes through the flow rate adjustment unit 6 from the
first space P1 to the second space P2. The rest of sweep gas flows into the second
flow path 12 through the inflow port d1 of the reactor 1. The sweep gas that has taken
in water vapor and absorbed the reaction heat in the second flow path 12 flows out
to the second space P2 through the outflow port d2 of the reactor 1. The sweep gas
that has passed through the flow rate adjustment unit 6 and the sweep gas that has
passed through the second flow path 12 join together in the second space P2 and are
discharged to the outside through the sweep gas exhaust port 3b.
[0057] In this manner, the reactor 1 can be cooled from the outside using the sweep gas
passing through the flow rate adjustment unit 6, as well as from the inside using
the sweep gas flowing through the second flow paths 12. In particular, due to the
sweep gas passing through the flow rate adjustment unit 6, the sweep gas can be inhibited
from being retained near the flow rate adjustment unit 6, and thus the cooling efficiency
from the outside can be improved without providing a special structure. Accordingly,
since the reaction heat generated due to the conversion reaction can be efficiently
removed, the conversion efficiency can be further improved.
[0058] Also, as shown in FIG. 5, in the side view of the reactor 1, the direction in which
the sweep gas flows from the first space P1 to the second space P2 via the flow rate
adjustment unit 6 is the same as the direction in which the sweep gas flows through
the second flow paths 12. Accordingly, the reactor 1 can be cooled from the outside
using the relatively cool sweep gas that has not passed through the inside of the
reactor 1, and thus the cooling efficiency from the outside can be further improved.
[0059] Note that, in FIG. 5, the sweep gas supply port 3a and the sweep gas exhaust port
3b formed in the housing 3 are disposed on a straight line intersecting the axial
center of the reactor 1 in the cross-sectional view. In this manner, since the lengths
of the flow paths of the sweep gas that flows from the sweep gas supply port 3a to
the sweep gas exhaust port 3b through the second flow paths 12 can be made the same,
uneven flow of the sweep gas can be suppressed. Note that the positional relationship
between the sweep gas supply port 3a and the sweep gas exhaust port 3b can be changed
as appropriate.
Modification of Embodiment
[0060] Although an embodiment of the present invention has been described above, the present
invention is not limited to the above embodiment, and various modifications can be
made without departing from the gist of the invention.
Modification 1
[0061] FIG. 6 is a cross-sectional view of a reactor module 2 shown in FIG. 5. FIG. 6 shows
a cross-section perpendicular to the axial center of the reactor 1.
[0062] As shown in FIG.6, a first extending direction in which the outflow slits 15 extend
in the reactor 1 is preferably inclined or orthogonal with respect to a sweep gas
discharging direction in which the sweep gas is discharged to the outside through
the sweep gas exhaust port 3b. Specifically, an angle θ1 of the first extending direction
with respect to the discharging direction is preferably 45° or more and 135° or less.
In this manner, uneven flow of the gas from the opening portions on both sides of
the outflow slits 15 to the sweep gas exhaust port 3b can be suppressed, and thus
uneven flow of the sweep gas can be suppressed.
[0063] FIG. 7 is a cross-sectional view of the reactor module 2 shown in FIG. 5. FIG. 7
shows a cross section perpendicular to the axial center of the reactor 1.
[0064] As shown in FIG.7, a second extending direction in which the inflow slits 14 extend
in the reactor 1 is preferably inclined or orthogonal with respect to a sweep gas
supply direction in which the sweep gas is supplied through the sweep gas supply port
3a. Specifically, an angle θ2 of the second extending direction with respect to the
supply direction is preferably 45° or more and 135° or less. In this manner, uneven
flow of the gas from the sweep gas supply port 3a to opening portions on both sides
of the inflow slits 14 can be suppressed, and thus uneven flow of the sweep gas can
be suppressed.
Modification 2
[0065] Although the separation membrane 30 is permeable to water vapor, which is a product
of the conversion reaction of the raw material gas to the liquid fuel in the above
embodiment, the present invention is not limited thereto. The separation membrane
30 may be permeable to the liquid fuel itself, generated through the conversion reaction
of the raw material gas to the liquid fuel. In this case as well, the reaction equilibrium
of the above formula (1) can be shifted to the product side.
[0066] Also, when the separation membrane 30 is permeable to the liquid fuel, even when
generating the liquid fuel through a reaction in which no water vapor is generated
(e.g., H
2 + CO ↔ CH
3OH), the reaction equilibrium can be shifted to the product side.
Modification 3
[0067] Although the air-permeable annular flow rate adjustment unit 6 is constituted by
the porous material in the above embodiment, there is no limitation thereto. The flow
rate adjustment unit 6 need only have a structure capable of causing the sweep gas
to pass through from the first space P1 to the second space P2.
[0068] Here, FIG. 8 is a cross-sectional view of the flow rate adjustment unit 6. As shown
in FIG. 8, the flow rate adjustment unit 6 can be constituted by a support member
61, a packing 62, a seal member 63, and a pressing member 64.
[0069] The support member 61 has an annular shape. The support member 61 is disposed surrounding
the reactor 1 (porous support body 10). The support member 61 supports the packing
62 and the seal member 63. A vent hole 61a is formed in the support member 61. The
vent hole 61a is in communication with the first space P1 and the second space P2.
The sweep gas flows from the first space P1 to the second space P2 via the vent hole
61a. The flow rate of the sweep gas can be adjusted as appropriate by changing the
size and shape of the vent hole 61a.
[0070] The packing 62 is an annular elastic member. The packing 62 is fixed to the support
member 61 with a fastening member 62a. The packing 62 is disposed between the support
member 61 and the housing 3. The packing 62 seals a gap between the support member
61 and the housing 3.
[0071] The seal member 63 is an annular gland packing. The seal member 63 can be constituted
by, for example, exfoliated graphite. The seal member 63 is disposed between the support
member 61 and the reactor 1 (porous support body 10). The seal member 63 is compressed
by the pressing member 64. The air permeability of the seal member 63 can be adjusted
by changing the pressing force of the pressing member 64. The sweep gas flows from
the first space P1 to the second space P2 via the seal member 63. The flow rate of
the sweep gas can be adjusted as appropriate by changing the compression force of
the pressing member 64.
[0072] The pressing member 64 is fixed to the support member 61 by a fastening member 64a.
The pressing member 64 presses the seal member 63. The pressing force of the pressing
member 64 can be adjusted as appropriate by changing the fastening amount of the fastening
member 64a.
[0073] In this manner, the flow rate adjustment unit 6 shown in FIG. 8 exhibits air permeability
due to the vent hole 61a and the seal member 63 of the support member 61 functioning
as the flow paths of the sweep gas.
[0074] Note that the flow rate adjustment unit 6 shown in FIG. 8 may have only one of the
vent hole 61a and the seal member 63.
Modification 4
[0075] Although a reactor module provided with a reactor has been described in the above
embodiment, the present invention can also be applied to a separation membrane module
provided with a separation filter. The separation filter has the same configuration
as the reactor 1 according to the above embodiment, except that the separation filter
has a separation membrane for separating a predetermined component from a mixed fluid.
[0076] In such a separation membrane module, in order to control the separation membrane
at an appropriate temperature, the separation membrane is to be heated or cooled by
causing the sweep gas to flow through the permeation side flow path in some cases.
In this case, as in the above embodiment, in the side view of the separation filter,
the direction in which the sweep gas flows from the first space P1 to the second space
P2 via the flow rate adjustment unit 6 is set the same as the direction in which the
sweep gas flows through the second flow paths 12. In this manner, the separation filter
can be efficiently cooled or heated from the outside using the sweep gas that has
not passed through the inside of the separation filter.
[0077] In the above embodiment, the temperature of the sweep gas is lower than the operation
temperature of the reactor 1. However, in the separation membrane module, in order
to cool the separation membrane, it is necessary to set the temperature of the sweep
gas lower than the temperature of the separation filter. On the other hand, in order
to heat the separation membrane, it is necessary to set the temperature of the sweep
gas higher than the temperature of the separation filter.
REFERENCE SIGNS LIST
[0078]
- 1
- Reactor
- 2
- Reactor module
- 3
- Housing
- 3a
- Sweep gas supply port
- 3b
- Sweep gas exhaust port
- 3c
- Raw material supply port
- 3d
- Liquid fuel exhaust port
- 4
- First seal portion
- 5
- Second seal portion
- 6
- Flow rate adjustment unit
- 10
- Porous support body
- 11
- First flow path
- e1
- Inflow port
- e2
- Outflow port
- 12
- Second flow path
- 13
- Cell
- 14
- Inflow slit
- d1
- Inflow port
- 15
- Outflow slit
- d2
- Outflow port
- 20
- Catalyst
- 30
- Separation membrane
- 40
- First seal portion
- 50
- Second seal portion